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The Levinthal paradox of the interactome

Peter Tompa1* and George D. Rose2


VIB Department of Structural Biology, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium

Jenkins Department of Biophysics, Johns Hopkins University, Baltimore, Maryland MD 21218

Received 6 September 2011; Revised 22 September 2011; Accepted 23 September 2011

DOI: 10.1002/pro.747
Published online 10 October 2011

Abstract: The central biological question of the 21st century is: how does a viable cell emerge
from the bewildering combinatorial complexity of its molecular components? Here, we estimate
the combinatorics of self-assembling the protein constituents of a yeast cell, a number so vast
that the functional interactome could only have emerged by iterative hierarchic assembly of its
component sub-assemblies. A protein can undergo both reversible denaturation and hierarchic
self-assembly spontaneously, but a functioning interactome must expend energy to achieve
viability. Consequently, it is implausible that a completely denatured cell could be reversibly
renatured spontaneously, like a protein. Instead, new cells are generated by the division of
pre-existing cells, an unbroken chain of renewal tracking back through contingent conditions
and evolving responses to the origin of life on the prebiotic earth. We surmise that this nondeterministic temporal continuum could not be reconstructed de novo under present conditions.
Keywords: interactome; proteinprotein interaction; Levinthal; protein folding; irreversibility;
assembly pathway; steady state; combinatorics

Protein folding, the spontaneous acquisition of
native conformation under physiological conditions,1
remains as one of the major unsolved problems in biological chemistry. The underlying search issue was
formulated persuasively by Cyrus Levinthal2 in a
back-of-the-envelope calculation, which demonstrated that a polypeptide chain could not arrive at
its native structure in biological real-time by random
search because conformational space is far too vast.
His formulation has come to be known as the Levinthal paradox, although for Levinthal it was no paradox at all but rather a demonstration that folding

Additional Supporting Information may be found in the online

version of this article.
Grant sponsor: Korea Research Council of Fundamental
Science and Technology (KRCF); Grant sponsor: FP7 Marie
Curie Initial Training Network; Grant number: 264257,
IDPbyNMR; Grant sponsor: FP7 Infrastructures; Grant number:
261863, BioNMR; Grant sponsors: National Science Foundation
and the Mathers Foundation
*Correspondence to: Peter Tompa, VIB Department of
Structural Biology, Vrije Universiteit Brussel, Pleinlaan 2, 1050
Brussels, Belgium. E-mail:


PROTEIN SCIENCE 2011 VOL 20:20742079

proceeds along preferred pathways. Levinthals calculation has influenced many current formulations
of the search problem in protein folding, see, for
example, Dill and Chan.3
Understanding how a protein acquires its native
structure, however, is only the initial search problem.
Successful cellular function depends upon subsequent
interactions with a host of other cellular constituents,
resulting in a complex network called the interactome. A comprehensive description of the interactome
has become the focus of recent ambitious highthroughput proteinprotein interaction studies.4,5
Unlike protein folding, self-assembly of the
interactome has not yet prompted such widespread
attention, and for understandable reasons. It is a
problem of bewildering complexity, far more challenging than the beguiling simplicity of two-state
proteins like ribonuclease that can self-assemble in
vitro.6 Where does one begin? Our goal here is to
show that assembly of the interactome in biological
real-time is analogous to folding in that the functional state is selected from a staggering number of
useless or potentially deleterious alternatives. In
particular, a simplified calculation is sufficient to
show that the number of distinguishable states of

C 2011 The Protein Society

Published by Wiley-Blackwell. V

the interactome exceeds comprehension. Consequently, the cell cannot self-organize by random assembly of its components. Instead, there must be
pathways of hierarchic self-organization that result
in functional modules, as proposed by Alberts.7
Here, we extend this proposition by incorporating
knowledge that the functional interactome requires
a continuous influx of energy for its generation and
maintenance. This requirement has significant
implications in evolution, physiology, pathology, and
synthetic biology.

Levinthal Paradox of the Interactome

Levinthals calculation2 assumed nine possible configurations for each /,w-pair in the backbone (three
staggered configurations for each rotatable bond,
like ethane), resulting in 9100  1095 possible conformations for a chain of 100 residues. Given the time
required for single bond rotations (picoseconds),
even a small protein that initiated folding by random search at the time of the big bang would still be
thrashing about today.8 The Levinthal estimate is
based on Florys simplifying assumption9 that each
/,w-pair is sterically independent of the others. That
assumption has been challenged,10,11 but the search
problem persists.
If the protein search problem seems perplexing,
the corresponding problem for a cell is bewildering.
Taking yeast as a model organism, approximately
4500 different proteins are expressed during log-phase
growth, each present in 50 to more than 106 copies
per cell, with a median value of about 3000 and a median length of about 400 residues  50 kDa molecular
weight.12 Assuming spherical shape and average density 1.1 g/cm3, the median protein would have a radius
and a surface area of 8692 A
2. Next, assume
of 26.3 A
the surface area of an average protein:protein inter 2, the equivalent of 22 interfacial
face is about 800 A
2.13 Also assume
residues, each contributing 36.4 A
that displacement by a residue or rotation by its diam 2 is repreeter (where each residues surface of 36.4 A
) would
sented by a circular patch, diameter 6.8 A
alter the specificity of interaction within each inter 2/36.4 A
2 239 possiface. This works out to be 8692 A
ble interface centers, with rotations producing 14.8
different orientations for each (again, assuming the
2, perimeter
interface is a circular patch of 800 A

100 A). In all, an average protein would have approximately 3540 distinguishable interfaces.
Assuming the simplest case that each of n proteins is present in a single copy in the proteome and
all proteins engage in pairwise interactions (Fig. 1),
the total number of possible distinct patterns of
interactions is:

Tompa and Rose


Figure 1. The number of possible interactomes increases

exponentially with proteome size. The number of possible
different states (patterns of pairwise interactions) of the
interactome increases exponentially with the number of its
constituent proteins. In the simple case of four proteins (A),
the number of possible different arrangements is only three.
Five proteins (B) may already engage in 15 different
pairwise interactions. The first pair (red-blue, red-purple,
red-yellow, red-green) is connected by a solid line, followed
by any of three possible secondary pairs (with connections
indicated by dotted lines), plus three remaining possibilities
(not illustrated) in which the first protein (red) is unpaired.
The theoretical number for n proteins is n!/2n/2  n/2!
(cf. text and Supporting Information), which for a realistic
interactome of 4500 proteins gives 107200 different

(for details of calculations, cf. Supporting Information). For n 4500, this is on the order of 107200, an
unimaginably large number; but a more realistic calculation is yet more complicated. With an average of
3540 distinct interfaces for a single protein, there
are 4500  3540 1.6  107 entities, resulting in
105.410 possible distinct interaction patterns (cf.
Supporting Information). If proteins are present in
3000 copies instead of a single copy, identical pairwise complexes of the same pair should not add to
multiplicity of interactions patterns; nevertheless,
the number of distinct interactomes increases further because different copies of the same protein can
engage in interactions with different partners at the
same time. In this case, the estimated number of
different interactomes is on the order of 107.910
(cf. Supporting Information).
Of course, there are additional complicating factors such as alternative splicing, post-translational
modifications, non-pairwise macromolecular interactions, incorrect complex formation that is adventitiously stable, and so forth. However, even neglecting such complications, the numbers preclude
formation of a functional interactome by trial and
error complex formation within any meaningful
span of time. This numerical exercise, a Levinthal
paradox of the interactome, is tantamount to a proof
that the cell does not organize by random collisions
of its interacting constituents. In analogy to protein
folding,14,15 an inescapable conclusion from these
numbers is that interactome assembly proceeds



along pathways and results in a hierarchy of functional modules.7 This conclusion is not altogether
surprising when the number of pairwise interactions
increases beyond a certain threshold, as shown
abstractly for random graphs by Erdos and Renyi16
and for scale-free real-world networks by Gavin et al.4

Hierarchic Assembly of the Interactome

At the level of relatively simple multiprotein complexes, such as the bacterial ribosome, effective and
spontaneous self-assembly can be observed in reconstitution experiments in vitro.17,18 In a series of classic papers, Nomura and coworkers have shown that
fully active 30S E. coli ribosome assembles from its
isolated components16S RNA and 21 purified proteins. This was a remarkable early demonstration
that components of the ribosome encode its assembly
pathway and final assembled state. Such self-assembling complexes represent fundamental modules in
the cellular hierarchy. In a similar vein, de novo synthesis of infectious poliovirus in a cell-free system
has been demonstrated.19 This impressive achievementconducted in an isolated environment, free
from extraneous interactions with cellular proteinsis akin to ribosomal self-assembly in both
complexity and compartmentalization.
Many subsequent observations of higher-level
hierarchic assembly in the interactome recapitulate
the early discovery of ribosomal self-assembly, underscoring the notion that the cell can be viewed as an
elaborate network of interlocking assembly lines, each
of which is composed of a set of large protein
machines.7 For example, protein synthesis is spatially
and temporally regulated in the cell. About three-quarter of mRNA molecules have non-random cellular
localization,20 ensuring that many proteins are made
where they are needed, and the sequenced timing of
their expression is apparent from the correlation
between interaction and expression profiles in yeast.21
Also, there is a range of spatial signals that target proteins to functionally relevant cellular sites of interaction, such as the nuclear export signal22 or the endoplasmic reticulum retrieval signal.23 In essence, a
complicated cellular sorting/trafficking and assembly
system, made up of membranous organelles, receptors,
membrane translocation devices, cytoskeletal tracks,
motor proteins, and accessory chaperones guides the
proper compartmentalization, localization, and assembly of proteins in the cell.2426 Here, we show that in
the absence of energy even this well developed infrastructure would be insufficient to account for the generation of the interactome, which requires a continuous expenditure of energy to maintain steady state.

Limitations of Spontaneous Assembly from

Isolated Proteins
Based on these observations that are consistent with
hierarchic self-assembly carefully guided by spatial



and temporal signals, it may seem that the interactome can and wouldform spontaneously from its
isolated components. In other words, there would be
a way to unboil the denatured cell, that is, to promote its assembly from a disassembled state, akin to
refolding a denatured protein.1 However, several
points suggest that this view is overly simple.
First, even spontaneous (re)folding, typical of
small proteins, is often irreversible in larger aggregation-prone proteins. The problem is far more
severe in the crowded environment of the cell, where
many proteins require chaperones and recombinant
proteins tend to aggregate. It is known that chaperone-assisted folding is an energy-requiring process,
but the prevailing interpretation is that the chaperone only acts as a catalyst that facilitates formation
of the folded state of the protein that could have
been attained spontaneously under dilute solution
conditions. However, if extrapolated to a macromolecular complex, this view may be too simplistic. The
ability of proteins to form prions27 and amyloids28
demonstrates that the physiologically relevant folded
state is probably not one of maximum stability,
although it may be the most kinetically accessible
metastable state. Consequently, Anfinsens thermodynamic hypothesis1 comes with a qualifying corollary, one that may well take precedence in the interactome. Upon initial consideration, misfolding
(misassembly) might seem to be an unlikely outcome
in the spontaneous assembly of macromolecular complexes, such as the ribosome, but this impression
cannot withstand closer scrutiny. Successful self-assembly conditions had to be carefully worked out for
the bacterial ribosome,17,29 and corresponding conditions are unattainable for the eukaryotic ribosome,
which requires as many as 200 accessory proteins
in vivo, most of them essential.30 Even lesscomplicated complexes, such as the nucleosome31 or
the proteasome,32 require assisted assembly in the
cell. Such examples illustrate a basic difference
between the in vitro assembly of 20 isolated components, each introduced in a specific order under controlled conditions, and their in vivo assembly amidst a
sea of competing components. The underlying problem
is well illustrated by calculations showing that physiological interactions are not necessarily the energetically dominant possibilities in the interactome.33
Over and above combinatorial complexity, there
is a fundamental chicken-and-egg dilemma: correct
interpretation of assembly signals and pathways
may require a prior network of interacting proteins,
that is, the interactome itself. For example, mRNA
localization requires the cytoskeleton, along which
transport can proceed.20 In turn, the cytoskeleton
requires prior organization, such as the microtubuleorganizing centers (MTOCs), for proper assembly,34
and transport along the cytoskeleton requires protein motors, large complexes themselves. Again, the

Levinthal Paradox of the Interactome

closely related bacterium. The spontaneous origination of a de novo cell has yet to be observed; all
extant cells are generated by the division of preexisting cells that provide the necessary template for
perpetuation of the interactome.
To illustrate the discontinuity between a viable
interactome and its isolated components, we postulate a minimum of three conceptually distinct zones
of differing complexity (Fig. 2):

Figure 2. The interactome cannot assemble from its

constituent proteins. Due to the incomprehensible number
of possible realizations and the energy needed for all
assembly mechanisms, we suggest a discontinuity between
a viable interactome and its isolated components, by
postulating three conceptually distinct zones of differing
complexity. Zone 1 (order, native state) corresponds to the
viable interactome in steady state, where fluctuations are
completely reversible. Excursion to zone 2 (disorder) due
to stress, disease, mutations, and large physiological
rearrangements can be reversed at the expense of
energy. Zone 3 (chaos) is vast and undifferentiated,
representing a lethal level of disorganization brought about
by extreme stress: current excursions into this zone are

nuclear export signal requires the presence and

operation of the nuclear pore complex for proper
operation.35 Although cellular function depends
upon the elaborate network of interlocking assembly lines,7 it cannot be established in the absence of
its own prior formation, a conundrum at the crux of
self-replicating life. In addition, the operation of all
these machines requires a continuous input of
energy, and therefore it is not feasible that the end
result (i.e., the functional interactome) could maintain steady-state conditions in an energy-independent fashion.
Perhaps the most profound conclusion to be
drawn from our calculations of combinatorial complexity is that the emergent interactome could not
have self-organized spontaneously from its isolated
protein components. Rather, it attains its functional
state by templating the interactome of a mother cell
and maintains that state by a continuous expenditure of energy. In the absence of a prior framework
of existing interactions, it is far more likely that
combined cellular constituents would end up in a
non-functional, aggregated state, one incompatible
with life. Even the recent successful creation of an
artificial bacterial cell36 only demonstrates that synthetic genetic material can be transplanted into the
cytoplasm (i.e., the viable interactome) of a very

Tompa and Rose

(i) Zone 1 (order, native state) corresponds to the viable interactome under normal, physiological conditions, defined as a collection of closely related
states generated by thermal fluctuations (dissociations/associations) around an equilibrium state. In
this zone, spontaneous assembly dominates and
fluctuations are completely reversible.
(ii) Zone 2 (disorder) is defined by reversible excursions from zone 1 owing to stress, disease, mutations, large physiological rearrangements such
as cell division, and so forth. In this zone, there
is somewhat less reversibility, but excursions
here can be reversed at the expense of energy
by a combination of pathways, compartments,
and chaperones.
(iii) Zone 3 (chaos) is vast and undifferentiated, representing the lethal level of disorganization
brought about by extreme stress, a level that
cannot be reversed by self-assembly mechanisms. An excursion into this zone is not reversible. Whereas zone 1 may represent a steady
state in some abstract interaction space, there
is no mechanism for reaching it from zone 3 in a
biologically relevant time frame.
An implicit consequence of this conceptual
model is that life would have traversed zone 3 at
least once. Presumably, early-earth life forms originated through an accumulation of changes of ever
increasing complexity, resulting eventually in photosynthetic prokaryotes. In this sense, extant assembly-pathways almost certainly echo their own evolutionary history, that is, a protein is guided to its
cellular destination along a route that was established at an earlier time and subsequently fortified
by other, similarly developed, interdependent cellular processes. Supporting evidence for this conclusion is provided by a recent mass-spectroscopy study
of the conservation and formation of the quaternary
structure of protein homomers.37 This study confirmed that structure alone is sufficient to infer both
the evolutionary and physical path of subunit assembly, an example of ontogeny recapitulates phylogeny at the cellular level.

Misfolding errors in proteins can cause assembly
errors that propagate across cellular pathways, with



opportunities for malfunction at each successive

level. At the level of individual molecules, protein
misfolding errors can produce non-native aggregated
states, with deleterious consequences to the cell.28
At the level of a pathway, assembly errors can lead
to disease-causing mis-localizations and mis-interactions. Typically, such processes are interrelated: misfolding can result in mis-interactions that terminate
in an aggregated dead-end.28 Such entanglement is
well illustrated by prions, infectious proteins that
can propagate in the cell by a self-sustaining autocatalytic conformational change, resulting in the formation of amyloid.27 From the perspective of a protein, the prion catastrophe is a misfolding disease,
while from the perspective of the interactome, it is a
mis-interaction disease.
It follows that there are many opportunities for
disease-associated mutations which can cause mislocalization and mis-interaction of proteins. Whereas
most monogenic disease-causing mutations promote
destabilization of protein structure,38 such mutations can also affect protein expression, translation,
transport, and localization.39 An instructive example
is primary hyperoxaluria (abnormally high oxalate
excretion). Approximately, one-third of such cases
are associated with a protein-sorting defect in hepatic L-alanine:glyoxylate aminotransferase (AGT).
The enzyme is peroxisomal under normal circumstances, but in disease it is mistargeted to mitochondria by mutations in its N-terminal region, which
generate an aberrant mitochondrial targeting
sequence that is misinterpreted by the mitochondrial
protein import machinery.40
Our view of the interactome may also provide
insight into chaperone action, which also functions
at both the protein folding and protein assembly
level. Indeed, the term chaperone was actually
coined for a protein-assisted assembly of the nucleosome.31 The existence of protein-assisted stabilization prompts the notion of a complementary process
of protein-inhibited destabilization, such as the
recently proposed nanny proteins, which prevent
degradation and improper interactions of their partner proteins.41 The chaperone system, which can
stabilize proteins and pathways against stress, is
itself subject to stress, and its breakdown under
overload conditions42 may also contribute to
The inability of the interactome to self-assemble
de novo imposes limits on efforts to create artificial
cells and organisms, that is, synthetic biology. In
particular, the stunning experiment of creating a
viable bacterial cell by transplanting a synthetic
chromosome into a host stripped of its own genetic
material36 has been heralded as the generation of a
synthetic cell43 (although not by the papers
authors). Such an interpretation is a misnomer,
rather like stuffing a foreign engine into a Ford and



declaring it to be a novel design. The success of the

synthetic biology experiment relies on having a recipient interactome in zone 1 (or, worst case, zone 2)
that has high compatibility with donor genetic material. The ability to synthesize an actual artificial cell
using designed components that can self-assemble
spontaneously still remains a distant challenge.

P.T. is indebted to Dr. and Mrs. Kalman Tompa for
helpful discussions on the combinatorial aspects of the
va Tudos (Institute of Enzymolinteractome and Dr. E
ogy, Hungarian Academy of Sciences, Budapest,
Hungary) for help in calculating large factorials.

1. Anfinsen CB (1973) Principles that govern the folding
of protein chains. Science 181:223230.
2. Levinthal C, How to fold graciously. In: DeBrunner
JTP, Munck E, Eds. (1969) Mossbauer spectroscopy in
biological systems. Allerton House, Monticello, Illinois:
University of Illinois Press, pp. 2224.
3. Dill KA, Chan HS (1997) From levinthal to pathways
to funnels. Nat Struct Biol 4:1019.
4. Gavin AC, Aloy P, Grandi P, Krause R, Boesche M,
Marzioch M, Rau C, Jensen LJ, Bastuck S, Dumpelfeld
B, Edelmann A, Heurtier MA, Hoffman V, Hoefert C,
Klein K, Hudak M, Michon AM, Schelder M, Schirle
M, Remor M, Rudi T, Hooper S, Bauer A, Bouwmeester
T, Casari G, Drewes G, Neubauer G, Rick JM, Kuster
B, Bork P, Russell RB, Superti-Furga G (2006) Proteome survey reveals modularity of the yeast cell machinery. Nature 440:631636.
5. Krogan NJ, Cagney G, Yu H, Zhong G, Guo X, Ignatchenko A, Li J, Pu S, Datta N, Tikuisis AP, Punna T, Peregrin-Alvarez JM, Shales M, Zhang X, Davey M,
Robinson MD, Paccanaro A, Bray JE, Sheung A, Beattie
B, Richards DP, Canadien V, Lalev A, Mena F, Wong P,
Starostine A, Canete MM, Vlasblom J, Wu S, Orsi C,
Collins SR, Chandran S, Haw R, Rilstone JJ, Gandi K,
Thompson NJ, Musso G, St Onge P, Ghanny S, Lam
MH, Butland G, Altaf-Ul AM, Kanaya S, Shilatifard A,
Oshea E, Weissman JS, Ingles CJ, Hughes TR, Parkinson J, Gerstein M, Wodak SJ, Emili A, Greenblatt JF
(2006) Global landscape of protein complexes in the
yeast Saccharomyces cerevisiae. Nature 440:637643.
6. Haber E, Anfinsen CB (1961) Regeneration of enzyme
activity by air oxidation of reduced subtilisin-modified
ribonuclease. J Biol Chem 236:422424.
7. Alberts B (1998) The cell as a collection of protein
machines: preparing the next generation of molecular
biologists. Cell 92:291294.
8. Kell DB, Welch GR (1991) No turning back: reductionism and biological complexity. Times Higher Educational Supplement, 9th August:p. 15.
9. Flory PJ (1969) Statistical mechanics of chain molecules. New York: Wiley.
10. Baldwin RL, Zimm BH (2000) Are denatured proteins
ever random coils. Proc Natl Acad Sci USA 97:
11. Pappu RV, Srinivasan R, Rose GD (2000) The Flory isolated-pair hypothesis is not valid for polypeptide
chains: implications for protein folding. Proc Natl Acad
Sci USA 97:1256512570.

Levinthal Paradox of the Interactome

12. Ghaemmaghami S, Huh WK, Bower K, Howson RW,

Belle A, Dephoure N, Oshea EK, Weissman JS (2003)
Global analysis of protein expression in yeast. Nature
13. Lo Conte L, Chothia C, Janin J (1999) The atomic
structure of proteinprotein recognition sites. J Mol
Biol 285:21772198.
14. Baldwin RL, Rose GD (1999) Is protein folding hierarchic? I. Local structure and peptide folding. Trends Biochem Sci 24:2633.
15. Baldwin RL, Rose GD (1999) Is protein folding hierarchic? II. Folding intermediates and transition states.
Trends Biochem Sci 24:7783.
16. Erdos P, Renya A (1960) On the evolution of random
graphs. Publ Math Inst Hungar Acad Sci 5:1761.
17. Held WA, Ballou B, Mizushima S, Nomura M (1974) Assembly mapping of 30 S ribosomal proteins from Escherichia coli. Further studies. J Biol Chem 249:31033111.
18. Held WA, Nomura M (1975) Escherichia coli 30 S ribosomal proteins uniquely required for assembly. J Biol
Chem 250:31793184.
19. Molla A, Paul AV, Wimmer E (1991) Cell-free, de novo
synthesis of poliovirus. Science 254:16471651.
20. Lecuyer E, Yoshida H, Parthasarathy N, Alm C, Babak
T, Cerovina T, Hughes TR, Tomancak P, Krause HM
(2007) Global analysis of mRNA localization reveals a
prominent role in organizing cellular architecture and
function. Cell 131:174187.
21. Ge H, Liu Z, Church GM, Vidal M (2001) Correlation
between transcriptome and interactome mapping data
from Saccharomyces cerevisiae. Nat Genet 29:482486.
22. Wen W, Meinkoth JL, Tsien RY, Taylor SS (1995) Identification of a signal for rapid export of proteins from
the nucleus. Cell 82:463473.
23. Nilsson T, Warren G (1994) Retention and retrieval in
the endoplasmic reticulum and the Golgi apparatus.
Curr Opin Cell Biol 6:517521.
24. Bhattacharyya RP, Remenyi A, Yeh BJ, Lim WA.
(2006) Domains, motifs, and scaffolds: the role of modular interactions in the evolution and wiring of cell signaling circuits. Annu Rev Biochem 75:655680.
25. Mellman I, Nelson WJ (2008) Coordinated protein sorting, targeting and distribution in polarized cells. Nat
Rev Mol Cell Biol 9:833845.
26. Bashor CJ, Horwitz AA, Peisajovich SG, Lim WA
(2010) Rewiring cells: synthetic biology as a tool to interrogate the organizational principles of living systems. Annu Rev Biophys 39:515537.
27. Prusiner SB (1998) Prions. Proc Natl Acad Sci USA 95:
28. Chiti F, Dobson CM (2006) Protein misfolding, functional amyloid, and human disease. Annu Rev Biochem

Tompa and Rose

29. Held WA, Mizushima S, Nomura M (1973) Reconstitution of Escherichia coli 30 S ribosomal subunits from
purified molecular components. J Biol Chem 248:
30. Strunk BS, Karbstein K (2009) Powering through ribosome assembly. RNA 15:20832104.
31. Laskey RA, Honda BM, Mills AD, Finch JT (1978)
Nucleosomes are assembled by an acidic protein which
binds histones and transfers them to DNA. Nature
32. Bedford L, Paine S, Sheppard PW, Mayer RJ, Roelofs J
(2010) Assembly, structure, and function of the 26S
proteasome. Trends Cell Biol 20:391401.
33. Wass MN, Fuentes G, Pons C, Pazos F, Valencia A
(2011) Towards the prediction of protein interaction
partners using physical docking. Mol Syst Biol 7:
34. Nigg EA, Raff JW (2009) Centrioles, centrosomes, and
cilia in health and disease. Cell 139:663678.
35. Patel SS, Belmont BJ, Sante JM, Rexach MF (2007)
Natively unfolded nucleoporins gate protein diffusion
across the nuclear pore complex. Cell 129:8396.
36. Gibson DG, Glass JI, Lartigue C, Noskov VN,
Chuang RY, Algire MA, Benders GA, Montague MG,
Ma L, Moodie MM, Merryman C, Vashee S, Krishnakumar R, Assad-Garcia N, Andrews-Pfannkoch C,
Denisova EA, Young L, Qi ZQ, Segall-Shapiro TH,
Calvey CH, Parmar PP, Hutchison CA, 3rd, Smith
HO, Venter JC (2010) Creation of a bacterial cell controlled by a chemically synthesized genome. Science
37. Levy ED, Boeri Erba E, Robinson CV, Teichmann SA
(2008) Assembly reflects evolution of protein complexes. Nature 453:12621265.
38. Yue P, Li Z, Moult J (2005) Loss of protein structure
stability as a major causative factor in monogenic disease. J Mol Biol 353:459473.
39. Shastry BS (2009) SNPs: impact on gene function and
phenotype. Methods Mol Biol 578:322.
40. Purdue PE, Allsop J, Isaya G, Rosenberg LE, Danpure
CJ (1991) Mistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to mitochondria in primary hyperoxaluria patients depends upon activation
of a cryptic mitochondrial targeting sequence by a
point mutation. Proc Natl Acad Sci USA 88:
41. Tsvetkov P, Reuven N, Shaul Y (2009) The nanny
model for IDPs. Nat Chem Biol 5:778781.
42. Csermely P (2001) Chaperone overload is a possible
contributor to civilization diseases. Trends Genet 17:
43. Wade N (2010) Researchers say they created a synthetic cell. The New York Times. New York.